7191-80-2

Usage

Appearance

Pale yellow to light brown crystalline solid
The physical state and color of the compound, describing its general appearance.

Melting point

80-84°C
The temperature range at which the compound transitions from a solid to a liquid state.

Chemical classification

Substituted aniline derivative
A classification based on the structure of the compound, indicating that it is derived from aniline (C6H5NH2) with a substitution of a chlorine atom.

Uses

Intermediate for the production of dyes, pigments, pharmaceuticals, and agrochemicals
The primary applications of the compound in various industries, highlighting its versatility as a chemical intermediate.

Hazardous properties

Toxic and potentially carcinogenic
The compound's potential health risks, emphasizing the need for careful handling and proper safety measures.

Handling precautions

Handle with care
A general recommendation to take necessary precautions when working with 1,2-Benzenediamine, N-[(2-chlorophenyl)methylene]- due to its hazardous nature.

Upstream product

• 89-98-5 2-chloro-benzaldehyde 
• 95-54-5 1,2-diamino-benzene 

Downstream Products

• 3574-96-7 2-(2-chlorophenyl)-1H-benzimidazole 
• 1536469-38-1 2-amino-3-(2-chlorophenyl)quinoxaline 

Relevant academic research and scientific papers

Chemoselective aerobic oxidation of 2-amino-N-benzylanilines into N-(2-aminophenyl)imines via a nitroxide-free copper catalysis

Chemoselective oxidative synthesis of N-(2-aminophenyl)imines from 2-amino-N-benzylanilines was accomplished through combined use of O2(air) and copper salt. This transformation was performed at room temperature, and the mild oxidation was efficient and chemoselective without using nitroxyl radicals and ligands.

Synthesis of 2-aminoquinoxalines via one-pot cyanide-based sequential reaction under aerobic oxidation conditions

A highly efficient synthesis of 2-aminoquinoxalines has been developed via the one-pot two-step cyanide-mediated sequential reactions of ortho-phenylenediamines with aldehydes under aerobic oxidation conditions. A variety of substrates, including aliphati

Microwave-assisted synthesis of substituted dibenzo[b,f][1,4]thiazepines, dibenzo[b,f][1,4]oxazepines, benzothiazoles, and benzimidazoles

A highly efficient synthesis for possessing 7-membered rings with two heteroatoms is described, using efficient microwave-assisted one-pot method to synthesize (substituted) dibenzo[b,f][1,4]thiazepines [1] and dibenzo[b,f][1,4]oxazepines [2] in high yields (up to 99%) by cyclocondensations of o-aminothiophenol or o-aminophenol with o-halobenzaldehydes, o-fluoroacetophenone, and o-fluorobenzophenone. In the absence of base, o-aminothiophenol reacted with o-halobenzaldehydes to afford benzothiazoles.

Ni nanoparticles: Mild and efficient catalyst for the chemoselective synthesis of 2-arylbenzimidazoles, 2-arylbenzothiazoles, and azomethines

(Chemical Equation Presented) A new and efficient method has been developed for the synthesis of biologically significant 2-arylbenzimidazoles, 2-arylbenzothiazoles, and azomethines using recyclable and inexpensive polyvinyl pyrrolidone (PVP)-stabilized Ni nanoparticles in ethylene glycol at room temperature in excellent yields. Copyright Taylor & Francis Group, LLC.